HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 136393672, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Methanone, [3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]phenyl- | HCID 1898376 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136393672 | HCID 136393672 | — |
Reaction Steps
12.4 g of 3,5-di-t-butyl-4-hydroxybenzophenone and 3.15 g of hydroxylamine hydrochloride were dissolved in 100 ml of ethanol, and with stirring, a solution of 2.77 g of potassium hydroxide in 20 ml of ethanol was added dropwise at room temperature. The mixture was then refluxed for 24 hours with stirring. After cooling, dichloromethane was added to the reaction mixture. The dichloromethane layer was separated, washed with water, and dried. The solvent was distilled off, and n-hexane was added to the residue. The precipitated crystals were collected by filtration, and recrystallized from ether/n-hexane to give 3,5-di-t-butyl-4-hydroxybenzophenone oxime.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04673692 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-5d3b0c9d259d4659b91eea4e916ecb27 |
| Source note | uspto-grants-1987_06 |